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首页> 外文期刊>International journal of legal medicine >The effects of extra PCR cycles when amplifying skeletal samples with the GlobalFiler (R) PCR Amplification Kit
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The effects of extra PCR cycles when amplifying skeletal samples with the GlobalFiler (R) PCR Amplification Kit

机译:扩增骨骼样品与GlobalFiler(R)PCR扩增套件扩增额外PCR循环的影响

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When samples with low amounts of DNA are amplified using short tandem repeats (STRs), stochastic effects such as allele and locus dropout or drop-in, allele imbalance, and increased stutter often occur making data interpretation more difficult. The most common approach to improving STR results from low template samples is to increase the number of PCR cycles. Although more alleles may be recovered, stochastic effects may be exaggerated resulting in more complicated STR profiles. This work reports the effect of additional PCR cycles (29 vs. 30, 31, and 32) on STR success from environmentally challenged bone and tooth samples using the GlobalFiler (R) DNA Amplification Kit (Thermo Fisher Scientific). In addition, we compared the efficiency of two DNA extraction kits for skeletal samples: QIAamp (R) DNA Investigator (QIAGEN) and PrepFiler (R) BTA (TM) Forensic DNA Extraction (Thermo Fisher Scientific) kits. Results showed that more DNA was recovered from samples using the PrepFiler (R) BTA (TM) kit; but regardless of the extraction method, the number of alleles detected and the peak heights both increased with an increase in PCR cycle number. Although more alleles were reported in almost all samples, the most notable improvement was observed in samples with the DNA template < 120 pg. A general increase in the number of PCR artifacts was detected in STR profiles generated using 30-32 cycles. Overall, this study provides supporting evidence that STR profile completeness and quality may be improved when low template skeletal samples are amplified with extra PCR cycles (up to 32 cycles) using the GlobalFiler (R) DNA Amplification Kit.
机译:当使用短串联重复(strs)扩增具有少量DNA的样品,随机效应如等位基因和基因座丢失或辍学,等位基因不平衡,并且通常会使数据解释更加困难。改善低模板样品的STR结果的最常见方法是增加PCR循环的数量。尽管可以回收更多的等位基因,但是可以夸大随机效应,从而产生更复杂的STR谱。该工作报告了使用Globalfiler(R)DNA扩增试剂盒(Thermo Fisher Scientific)的额外PCR循环(29 vs.31和32)对来自无害环境挑战的骨和牙齿样品的STR成功的影响。此外,我们将两种DNA提取试剂盒的效率与骨骼样品进行了比较:QIAAMP(R)DNA调查仪(QIAGEN)和预备液(R)BTA(TM)法医DNA提取(Thermo Fisher Scientific)试剂盒。结果表明,使用Prepfiler(R)BTA(TM)试剂盒从样品中回收更多DNA;但无论提取方法如何,检测到的等位基因数量和峰值高度都随PCR循环数的增加而增加。尽管在几乎所有样品中报道了更多的等位基因,但在具有DNA模板<120 pg的样品中观察到最值得注意的改进。在使用30-32个循环产生的STR谱中检测到PCR伪影数的一般增加。总的来说,该研究提供了支持证据,即使用Globalfiler(R)DNA扩增试剂盒用额外的PCR循环(最多32个循环)扩增了低模板骨骼样本,可以提高str轮廓完整性和质量。

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